Manuela Pendziwiat

3.9k citations
21 papers · 399 · h-index 12

Impact in

Papers in

    • Genetics and Neurodevelopmental Disorders 8
    • Genomics and Rare Diseases 6
    • Ion channel regulation and function 2
    • Ubiquitin and proteasome pathways 1
    • DNA Repair Mechanisms 1

Manuela Pendziwiat

21 papers receiving 395 citations

Peers

Manuela Pendziwiat
Comparison fields: 5 of 69
  • Psychiatry and Mental health 68
  • Cell Biology 71
  • Cellular and Molecular Neuroscience 65
  • Neurology 47
  • Genetics 80
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Citations per year

Countries citing papers authored by Manuela Pendziwiat

Since Specialization
Citations

This map shows the geographic impact of Manuela Pendziwiat's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Manuela Pendziwiat with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Manuela Pendziwiat more than expected).

Fields of papers citing papers by Manuela Pendziwiat

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Manuela Pendziwiat. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Manuela Pendziwiat. The network helps show where Manuela Pendziwiat may publish in the future.

Co-authors

The 25 scholars most cited alongside Manuela Pendziwiat, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Manuela Pendziwiat Line = papers co-authored together Manuela Pendziwiat links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 21 papers — load more, or switch the sort, to bring in the rest.

#Work
1 201392
2 201340
3 201436
4 201636
5 201027
6 202022
7 202219
8 201719
9 202017
10 201914
11 201613
12 201811
13 202010
14 202210
15 20158
16 20158
17 20217
18 20224
19 20213
20 20232

About Manuela Pendziwiat

Manuela Pendziwiat is a scholar working on Genetics, Molecular Biology, Neurology, Psychiatry and Mental health and Cell Biology, having authored 21 papers that have together received 399 indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (8 papers), Genomics and Rare Diseases (6 papers), Epilepsy research and treatment (5 papers), Parkinson's Disease Mechanisms and Treatments (3 papers), Ion channel regulation and function (2 papers), Ubiquitin and proteasome pathways (1 paper), Alzheimer's disease research and treatments (1 paper) and DNA Repair Mechanisms (1 paper). The work is most often cited by research in Psychiatry and Mental health (68 citations), Cell Biology (71 citations), Cellular and Molecular Neuroscience (65 citations), Neurology (47 citations) and Genetics (80 citations). Manuela Pendziwiat has collaborated with scholars based in Germany, United States and Israel. Frequent co-authors include Gregor Kuhlenbäumer, Ingo Helbig, Zaid Afawi, Silke Appenzeller, Kaifeng Zhou, Jonathan R. Bowen, Xiaobo Bai, Charles V. Sindelar, Elias T. Spiliotis and Inken Lorenzen. Their work appears in journals such as Epilepsia, The American Journal of Human Genetics, Journal of Neurology, Frontiers in Genetics and Cytoskeleton.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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